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[Pharmaceutical Verification of Chemotherapy-induced Adverse Events]
1Department of Clinical Pharmaceutics & Therapeutics, Faculty of Pharmaceutical Sciences, Hokkaido University of Science.
Abstract:
Managing adverse events is important for optimizing cancer treatment and ensuring high patient satisfaction. Studies have assessed (1) anti-epidermal growth factor receptor (EGFR) monoclonal antibody-induced skin toxicities, (2) development of severe neutropenia by renally excreted anticancer drugs in patients with renal impairment (RI), and (3) pharmaceutical care in the treatment of immune checkpoint inhibitors (ICIs). We identified liver metastasis as a risk factor and preemptive systemic antibiotic administration with anti-inflammatory effect as a preventive factor for grade ≥2 overall skin toxicities in anti-EGFR treatment for metastatic colorectal cancer (mCRC). Additional prophylactic topical steroids to systemic minocycline significantly prevented grade ≥2 rashes, but did not mitigate overall skin toxicities. Patients receiving trifluridine/tipiracil (FTD/TPI)-based chemotherapy for mCRC were assessed, resulting in significantly higher early severe neutropenia development among patients with RI. Additionally, we assessed the impact of RI on severe neutropenia development in carboplatin+pemetrexed-based chemotherapy for thoracic cancer. Consequently, severe neutropenia in the first cycle and all-treatment cycles was significantly more confirmed in patients with RI. We assessed the usefulness of pharmaceutical interventions in ICI treatment, which suggested that pharmaceutical care may improve quality of outpatient ICI treatment, and pharmaceutical intervention during the first three months after initiation of ICI treatment is crucial. Our studies have found clinically important outcomes that support the provision of less onerous chemotherapy.
Insights
Managing cancer treatment side effects is key. This study found liver metastasis increases skin toxicity risk with anti-EGFR therapy and renal impairment worsens neutropenia with chemotherapy, highlighting areas for improved patient care.
Area of Science:
- Oncology
- Pharmacology
- Clinical Pharmacy
Background:
- Optimizing cancer treatment and patient satisfaction requires effective management of adverse events.
- Studies have investigated anti-epidermal growth factor receptor (EGFR) toxicities, neutropenia in renal impairment (RI), and pharmaceutical care for immune checkpoint inhibitors (ICIs).
Purpose of the Study:
- To identify risk and preventive factors for skin toxicities in anti-EGFR therapy for metastatic colorectal cancer (mCRC).
- To assess the impact of RI on severe neutropenia development in patients receiving trifluridine/tipiracil (FTD/TPI) and carboplatin+pemetrexed chemotherapy.
- To evaluate the role of pharmaceutical care in optimizing outpatient ICI treatment.
Main Methods:
- Retrospective analysis of patients with mCRC undergoing anti-EGFR treatment to identify skin toxicity risk factors.
- Analysis of neutropenia development in patients with RI receiving FTD/TPI or carboplatin+pemetrexed chemotherapy.
- Assessment of pharmaceutical interventions in patients receiving ICIs.
Main Results:
- Liver metastasis was a risk factor for grade ≥2 skin toxicities in anti-EGFR therapy; preemptive antibiotics showed preventive effects.
- Topical steroids with minocycline prevented grade ≥2 rashes but not overall skin toxicities.
- Patients with RI had significantly higher early and overall severe neutropenia with FTD/TPI and carboplatin+pemetrexed chemotherapy.
- Pharmaceutical care may improve outpatient ICI treatment quality, with early intervention being crucial.
Conclusions:
- Clinically important outcomes were identified to support less burdensome chemotherapy regimens.
- Findings emphasize the need for tailored management of toxicities based on patient factors like RI and specific cancer types.
- Proactive pharmaceutical interventions are vital for enhancing cancer treatment outcomes and patient safety.
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